nemaline myopathy 3 (Q32144822)
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nemaline myopathy that has material basis in homozygous, compound heterozygous, or heterozygous mutation in the ACTA1 gene on chromosome 1q42
- NEM3
- nemaline myopathy 3, autosomal dominant or recessive
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | nemaline myopathy 3 |
nemaline myopathy that has material basis in homozygous, compound heterozygous, or heterozygous mutation in the ACTA1 gene on chromosome 1q42 |
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Statements
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C129870
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Identifiers
1 reference
1 reference